I just watched the movie All Is Lost, starring Robert Redford. It’s not the best movie, pretty sad, a bit slow, and all about survival without the hoped for character developement.
What I did get from the movie was that it could be an accurate depiction of life with chronic illness.
Watching Redford’s character struggle to survive kept making me think of my own struggle with chronic headache.
As he conquers a new problem you are filled with hope that he might just survive.
The same happens to us all while fighting our headaches. Each new medicine gives a new sense of hope.
I won’t spoil the ending, but I do hope your journey to wellness isn’t as trying as the character’s journey in All Is Lost.
Here’s my neuro answering commonly asked questions in video.
Watch and enjoy…
I myself wonder if he is a Dr. Who fan, and if that would qualify as a frequently asked question.
I found this article from Medical News Today quite interesting. Although it addresses cluster headache not my specific headache, whatever that diagnosis may turn out to be, any news of new treatment options is good news.
I considered having a neurostimulator implanted last year. My insurance denied the claim and I couldn’t afford to proceed. This smaller device implanted orally would make that type of treatment both easier and less expensive.
It hasn’t been approved for use in the U.S. yet. Hopefully they will have few road blocks on the way to approval and their success will inspire others to push for research in this type of headache treatment.
Another article, this time from Head Wise, points to research started last summer that may lead to portable, non-invasive neurostimulation treatment.
It’s great to see progress being made. I look forward to something working for me!